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Autoradiographic Visualization of G Protein-Coupled Receptors in Brain

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Receptor and Ion Channel Detection in the Brain

Part of the book series: Neuromethods ((NM,volume 110))

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Abstract

In this chapter, two in vitro techniques applied to study the anatomical localization of a receptor are revised: firstly, the receptor binding assay in sections, a technique to assess the location and distribution of a receptor in the tissue (descriptive and anatomical information), and, secondly, the [35S]GTPγS-binding assay also in tissue slices, which allows the quantification of the level of G protein activation by a specific GPCR’s agonist. The latter technique provides additional information about the coupling efficacy of a receptor to G proteins (functional autoradiography), thus enabling the study of the first step in the intracellular signaling pathway after the receptor activation. Both techniques are basically performed for the in vitro autoradiographic visualization of receptors in tissue slices obtained from animal or human postmortem samples.

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References

  1. Pazos A, Palacios JM (1985) Quantitative autoradiographic mapping of serotonin receptors in the rat brain. I. Serotonin-1 receptors. Brain Res 346:205–230

    Article  CAS  PubMed  Google Scholar 

  2. Castro ME, Diaz A, Del Olmo E, Pazos A (2003) Chronic fluoxetine induces opposite changes in G protein coupling at pre and postsynaptic 5-HT1A receptors in rat brain. Neuropharmacology 44:93–101

    Article  PubMed  Google Scholar 

  3. Happe HK, Bylund DB, Murrin LC (2001) Agonist-stimulated [35S]GTPgammaS autoradiography: optimization for high sensitivity. Eur J Pharmacol 422(1–3):1–13

    Article  CAS  PubMed  Google Scholar 

  4. Sim LJ, Selley DE, Childers SR (1995) In vitro autoradiography of receptor-activated G proteins in rat brain by agonist-stimulated guanylyl 5´-[γ-[35S]thio]-triphosphate binding. Proc Natl Acad Sci U S A 92:7242–7246

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Sóvágó J, Dupuis DS, Gulyás B, Hall H (2001) An overview on functional receptor autoradiography using [35S]GTPγS. Brain Res Rev 38:149–164

    Article  PubMed  Google Scholar 

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Acknowledgments

This work was supported by Ministerio de Ciencia, SAF07-61862, Ministerio de Economía y Competitividad SAF2011-25020, and Instituto de Salud Carlos III.

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Correspondence to Elena Castro .

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© 2016 Springer Science+Business Media New York

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Vidal, R., Linge, R., Castillo, M.J., Amigó, J., Valdizán, E.M., Castro, E. (2016). Autoradiographic Visualization of G Protein-Coupled Receptors in Brain. In: Luján, R., Ciruela, F. (eds) Receptor and Ion Channel Detection in the Brain. Neuromethods, vol 110. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-3064-7_11

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  • DOI: https://doi.org/10.1007/978-1-4939-3064-7_11

  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-3063-0

  • Online ISBN: 978-1-4939-3064-7

  • eBook Packages: Springer Protocols

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